Vasopressin is used to treat diabetes insipidus, GI hemorrhage, and esophageal varices. It works by increasing water reabsorption in the kidneys, constricting blood vessels, and causing contraction of the intestines, gallbladder, and bladder. Doses vary depending on the condition. Side effects include increased blood pressure, arrhythmias, and abdominal cramps.
Vasopressin is used to treat diabetes insipidus, GI hemorrhage, and esophageal varices. It works by increasing water reabsorption in the kidneys, constricting blood vessels, and causing contraction of the intestines, gallbladder, and bladder. Doses vary depending on the condition. Side effects include increased blood pressure, arrhythmias, and abdominal cramps.
Vasopressin is used to treat diabetes insipidus, GI hemorrhage, and esophageal varices. It works by increasing water reabsorption in the kidneys, constricting blood vessels, and causing contraction of the intestines, gallbladder, and bladder. Doses vary depending on the condition. Side effects include increased blood pressure, arrhythmias, and abdominal cramps.
Let’s go ahead and understand the pharmacology of Vasopressin.
Vasopressin is used in the treatment of diabetes insipidus, GI hemorrhage and esophageal varices. In some cases, it is reported to show benefits in vasodilatory shock. Let’s see the mechanism of action. Vasopressin is a posterior pituitary hormone which can also be prepared or extracted synthetically from animals. It increases tubular reabsorption of water thereby exerts direct antidiuretic action on the kidney reabsorption. It also acts by constricting the peripheral blood vessels and causes the smooth muscle of the intestine, gallbladder and urinary bladder to contract. In case of diabetes insipidus, vasopressin of 5 to 10 units is administered. For gastrointestinal hemorrhage, 0.2 to 0.4 microgram per minute is prescribed. In case of vasodilatory shock, 0.01 to 0.1 microgram per minute is prescribed. Monitor serum and urine sodium, urine and serum osmolality, urine output, fluid input and output, blood pressure, heart rate, while administering vasopressin. The adverse effects of vasopressin include increased blood pressure, bradycardia, arrhythmias, venous thrombosis, abdominal cramps, tremor, angina, cardiac arrest, bronchoconstriction. Let’s take a closer look at the pharmacology of Vecuronium. Vecuronium provides skeletal muscle relaxation during surgery or mechanical ventilation. It has no amnestic or analgesic properties. Vecuronium blocks nicotinic receptors by competitively binding to it and thereby preventing acetylcholine binding. This results in skeletal muscle relaxation. Talking about the dose of administration, Vecuronium is usually administered at a dose of 80 to 100 microgram per kilogram is given by IV or Intravenous. Maintenance dose: 20 to 30 microgram per kilogram by injection or by infusion at 0.8 to 1.4 microgram per kilogram per min. Vasopressin Monitor blood pressure, heart rate, peripheral nerve stimulation wile administering vecuronium. The adverse effects of vecuronium are urticaria, bronchospasm, a potential for prolonged paralysis or weakness with the prolonged administration (systemic steroids), difficulty in breathing, swelling of the face, irregular heartbeat, swelling and redness at the site of injection.